FDA Inspection 1071915 — BAROnova Inc.

BAROnova Inc. — FEI 3012573149

The FDA completed an inspection of BAROnova Inc. on Sep 27, 2018 in San Carlos, CA. The inspection was classified NAI (No Action Indicated — no objectionable conditions were found). Product area: Devices.

Inspection Details

Classification
No Action Indicated (NAI)
End Date
Sep 27, 2018
Fiscal Year
2018
Product Type
Devices
Project Area
Bioresearch Monitoring
Location
San Carlos, CA (United States)

Additional Details

Sponsor, Contract Research Organization